Olympia Pharmacy recalls T-105 vials due to improper investigation of environmental and personnel monitoring deviations before October 2021. Affected vials have specific NDC numbers and batch dates.
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
Olympia Pharmacy is recalling T-105 vials that contain papaverine, phentolamine, and PGE. The recall is due to CGMP deviations where monitoring issues weren't properly investigated before October 2021. This could lead to unsafe drug production if not addressed.
The recall is for vials produced before October 2021 that had environmental and personnel monitoring issues not properly investigated. This could mean the vials were contaminated or not safe for use, but the exact risk isn't specified in the notice.
People who have the specific T-105 vials with NDC numbers 73198-0005-10, 73198-0005-05, or 73198-0005-03. Patients using these vials for medical purposes are most at risk.
Check for vials labeled T-105 with papaverine 30mg/mL, phentolamine 1mg/ml, and PGE 10mcg/ml. The NDC numbers are 73198-0005-10, 73198-0005-05, or 73198-0005-03. The vials were sold with specific batch dates and expiration dates.
Identify the NDC number and batch date on the vial to confirm if it's affected.
The recall is due to CGMP deviations where environmental and personnel monitoring issues weren't properly investigated before October 2021.
The official notice doesn't specify a remedy, so contact Olympia Pharmacy directly for guidance.
Yes, affected vials have batch dates like D41412 (BUD: 4/22/2022) or F42B21 (BUD: 6/21/2022).
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0799-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0799-2022 from Olympia Pharmacy. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
